| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084268-37084600 | Common:5; Rare:124 | ||||
| chr2:37156745-37157174 | Common:4; Rare:138 | ||||
| chr2:37196394-37196734 | Common:5; Rare:119 | ||||
| chr2:37197073-37197203 | Rare:30 | ||||
| chr2:37231308-37231393 | Common:1; Rare:42 | ||||
| chr2:37231486-37231790 | Common:6; Rare:167; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37231951-37232003 | Rare:14 | ||||
| chr2:37324185-37324268 | Common:1; Rare:12 | ||||
| chr2:37324323-37324457 | Rare:43 | ||||
| chr2:37324633-37324985 | Common:1; Rare:131 | ||||
| chr2:37345040-37345133 | Rare:23 | ||||
| chr2:37671511-37671755 | Common:1; Rare:100 | ||||
| chr2:37672000-37672333 | Common:5; Rare:89 | ||||
| chr2:37672405-37672783 | Common:6; Rare:117 | ||||
| chr2:37672792-37672920 | Common:2; Rare:22 |